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Genetics of melanoma predisposition
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12789280
retrieved
31 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Genetics of melanoma predisposition.
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12789280
retrieved
31 July 2017
author name string
Nicholas K Hayward
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12789280
retrieved
31 July 2017
language of work or name
English
0 references
publication date
1 May 2003
1 reference
stated in
Europe PubMed Central
PubMed ID
12789280
retrieved
31 July 2017
published in
Oncogene
1 reference
stated in
Europe PubMed Central
PubMed ID
12789280
retrieved
31 July 2017
volume
22
1 reference
stated in
Europe PubMed Central
PubMed ID
12789280
retrieved
31 July 2017
issue
20
1 reference
stated in
Europe PubMed Central
PubMed ID
12789280
retrieved
31 July 2017
page(s)
3053-3062
1 reference
stated in
Europe PubMed Central
PubMed ID
12789280
retrieved
31 July 2017
exact match
https://scigraph.springernature.com/pub.10.1038/sj.onc.1206445
0 references
cites work
Sporadic multiple primary melanoma cases:CDKN2Agermline mutations with a founder effect
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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Familial cutaneous malignant melanoma and tumors of the nervous system. A hereditary cancer syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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Geographical variation in the penetrance of CDKN2A mutations for melanoma
1 reference
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reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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Glutathione S-transferase M1 and T1 polymorphisms: susceptibility to colon cancer and age of onset
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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Human CYP2D6 gene polymorphism in Slovene cancer patients and healthy controls
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13.
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
based on heuristic
inferred from DOI database lookup
A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genotype-Phenotype Relationships in U.S. Melanoma-Prone Families With CDKN2A and CDK4 Mutations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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Evidence for variable selective pressures at MC1R
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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inferred from DOI database lookup
Glutathione S-transferase GSTM1 phenotypes and protection against cutaneous tumours
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
based on heuristic
inferred from DOI database lookup
Susceptibility to melanoma: influence of skin type and polymorphism in the melanocyte stimulating hormone receptor gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
based on heuristic
inferred from DOI database lookup
A polymorphism in the agouti signaling protein gene is associated with human pigmentation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A familial syndrome with cutaneous malignant melanoma and cerebral astrocytoma.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair Color
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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inferred from DOI database lookup
Loss of p16Ink4a confers susceptibility to metastatic melanoma in mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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inferred from DOI database lookup
Phenotype of glutathione S-transferase Mu (GSTM1) and susceptibility to malignant melanoma. MMM group. Multidisciplinary Malignant Melanoma Group
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Patients with both pancreatic adenocarcinoma and melanoma may harbor germline CDKN2A mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isozyme variation in Larrea ameghinoi and Larrea nitida (Zygophyllaceae): genetic diversity and its bearing on their relationship
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
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7 January 2021
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inferred from DOI database lookup
Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CDKN2A mutations in multiple primary melanomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
G2 phase cell cycle arrest in human skin following UV irradiation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CDKN2A germline splicing mutation affecting both p16ink4 and p14arf RNA processing in a melanoma/neurofibroma kindred
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Screening of germline mutations in the CDKN2A and CDKN2B genes in Swedish families with hereditary cutaneous melanoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Haplotype analysis of two recurrentCDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A melanoma-associated germline mutation in exon 1beta inactivates p14ARF.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of G1/S checkpoint regulators in metastatic melanoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glutathione S-transferase GSTM1 null genotype is not overrepresented in Australian patients with nevoid basal cell carcinoma syndrome or sporadic melanoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human pigmentation genetics: the difference is only skin deep
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline CDKN2A mutations in childhood melanoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Relationship between the debrisoquine hydroxylase polymorphism and cancer susceptibility.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two p16 (CDKN2A) germline mutations in 30 Israeli melanoma families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial tumor syndrome associated with a germline nonfunctional p16INK4a allele
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.ONC.1206445
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/SJ.ONC.1206445
1 reference
stated in
Europe PubMed Central
PubMed ID
12789280
retrieved
31 July 2017
Dimensions Publication ID
1044380080
0 references
PubMed ID
12789280
1 reference
stated in
Europe PubMed Central
PubMed ID
12789280
retrieved
31 July 2017
ResearchGate publication ID
10723680
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